Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 66589142 | HCID 66589142 | — |
| Product | HCID 66589107 | HCID 66589107 | 84% |
Reaction Steps
Next, 226 mL of benzyl alcohol was cooled to 0° C. and 19.5 g (164 mmol) of thionyl chloride was added dropwise. After stirring for 15 minutes, 21.2 g (62.4 mmol) of 2-(N-benzyloxycarbonylamino)-4-phosphonobutanoic acid monosodium salt was added and stirred at room temperature for 20 hours after the ice bath was removed. Completion of the reaction was confirmed by TLC (BuOH/AcOH/H2O=5:2:2, 254 nm). Benzyl alcohol was removed by vacuum distillation at 70° C. using a vacuum pump. The obtained oily residue was extracted by 300 mL of ethyl acetate and insoluble sodium chloride was removed by filtration. After being washed with 50 mL of water three times, the filtrate was dried over anhydrous sodium sulfate. After the solvent was removed by vacuum distillation, 300 mL of diethyl ether was added, seed crystals were added and the mixture stirred vigorously, and the product was crystallized from product mixture was partially dissolved in the ether, benzyl 2-(N-benzyloxycarbonylamino)-4-phosphonobutanoate (21.2 g, yield 84%) was obtained as white powder-like crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129557B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-b28ed03db873461ebecef2019d6ac834 |
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| Source note | uspto-grants-2012_03 |
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